A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034522



Internal ID19123744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40326413..40342133hg38UCSC Ensembl
Innerchr8:40183932..40199652hg19UCSC Ensembl
Innerchr8:40303089..40318809hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3815721
hg1915721
hg1815721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7184n100
Supporting Variantsnssv3687238
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034522
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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